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dbVar

Database of genomic structural variation

nsv5575771

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:528

Publication(s):Ebert et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 153 SVs from 40 studies. See in: genome view

Submitted genomic113,602,185-113,602,712

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5575771	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	113,602,185	113,602,712
nsv5575771	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	114,359,762	114,360,289

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17107876	deletion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17107876	Submitted genomic		NC_000002.12:g.113 602185_113602712de lC	GRCh38 (hg38)		NC_000002.12	Chr2	113,602,185	113,602,712
nssv17107876	Remapped	Perfect	NC_000002.11:g.114 359762_114360289de lC	GRCh37.p13	First Pass	NC_000002.11	Chr2	114,359,762	114,360,289

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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